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- source_evidence_literature type ECO_0000212 NP613788.RAKJGR-ddEqZWweZ_-0yNolbaI-IGl4cfrgcOiRl3xu74130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP613788.RAKJGR-ddEqZWweZ_-0yNolbaI-IGl4cfrgcOiRl3xu74130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP613788.RAKJGR-ddEqZWweZ_-0yNolbaI-IGl4cfrgcOiRl3xu74130_provenance.
- NP613788.RAKJGR-ddEqZWweZ_-0yNolbaI-IGl4cfrgcOiRl3xu74130_assertion description "[Genes causing nonsyndromic autosomal recessive deafness (DFNB12) and deafness associated with retinitis pigmentosa and vestibular dysfunction (USH1D) were previously mapped to overlapping regions of chromosome 10q21-q22.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP613788.RAKJGR-ddEqZWweZ_-0yNolbaI-IGl4cfrgcOiRl3xu74130_provenance.
- NP613788.RAKJGR-ddEqZWweZ_-0yNolbaI-IGl4cfrgcOiRl3xu74130_assertion evidence source_evidence_literature NP613788.RAKJGR-ddEqZWweZ_-0yNolbaI-IGl4cfrgcOiRl3xu74130_provenance.
- NP613788.RAKJGR-ddEqZWweZ_-0yNolbaI-IGl4cfrgcOiRl3xu74130_assertion SIO_000772 11090341 NP613788.RAKJGR-ddEqZWweZ_-0yNolbaI-IGl4cfrgcOiRl3xu74130_provenance.
- NP613788.RAKJGR-ddEqZWweZ_-0yNolbaI-IGl4cfrgcOiRl3xu74130_assertion wasDerivedFrom befree-20140225 NP613788.RAKJGR-ddEqZWweZ_-0yNolbaI-IGl4cfrgcOiRl3xu74130_provenance.
- NP613788.RAKJGR-ddEqZWweZ_-0yNolbaI-IGl4cfrgcOiRl3xu74130_assertion wasGeneratedBy ECO_0000203 NP613788.RAKJGR-ddEqZWweZ_-0yNolbaI-IGl4cfrgcOiRl3xu74130_provenance.
- befree-20140225 importedOn "2014-02-25" NP613788.RAKJGR-ddEqZWweZ_-0yNolbaI-IGl4cfrgcOiRl3xu74130_provenance.